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Kliniske studier på 22q13.3 Slettingssyndrom
Totalt 22 resultater
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UMC UtrechtChildren's Hospital of Philadelphia; Netherlands Brain FoundationUkjentKromosom 22q11.2 delesjonssyndromForente stater, Nederland
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Hôpital le VinatierRekruttering
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University of Geneva, SwitzerlandFullført22q11.2 SlettingssyndromSveits
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Hôpital le VinatierAvsluttet
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Albert Einstein College of MedicineNational Heart, Lung, and Blood Institute (NHLBI)RekrutteringDiGeorge syndrom | 22q11.2 SlettingssyndromForente stater
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University of Geneva, SwitzerlandAvsluttet22q11.2 SlettingssyndromSveits
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Mahidol UniversityFullført22q11.2 Slettingssyndrom | ImmundefektThailand
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Stephan EliezRekrutteringtACS | 22Q11 delesjonssyndromSveits
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Zynerba Pharmaceuticals, Inc.Fullført22Q delesjonssyndromForente stater, Australia
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State University of New York - Upstate Medical...Albert Einstein College of MedicineFullført
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Aevi Genomic Medicine, LLC, a Cerecor companyFullført22q11.2 SlettingssyndromForente stater
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UMC UtrechtEindhoven University of TechnologyRekruttering22q11.2 Slettingssyndrom | Ungdoms idiopatisk skolioseNederland
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Duke UniversityNational Institute of Mental Health (NIMH); University of Pittsburgh; Harvard...Fullført
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Hôpital le VinatierRekruttering22q11.2 SlettingssyndromFrankrike
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Clinical Research Associates, LLCRekruttering16P11.2 SlettingssyndromForente stater
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University Hospital TuebingenRekruttering
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Icahn School of Medicine at Mount SinaiNational Institute of Mental Health (NIMH)FullførtPhelan-McDermid syndrom | 22q13 delesjonssyndromForente stater
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The Champ FoundationChildren's Hospital of Philadelphia; The Cleveland ClinicRekrutteringPearson syndrom | Enkelt store mitokondrielle DNA-slettingssyndromer (SLSMDS)Forente stater
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RTI InternationalUniversity of North Carolina, Chapel HillPåmelding etter invitasjonTuberøs sklerose | Downs syndrom | Duchenne muskeldystrofi | Prader-Willi syndrom | Fragilt X-syndrom | Rett syndrom | Turners syndrom | Williams syndrom | Angelman syndrom | Kromosom 22q11.2 delesjonssyndrom | Klinefelters syndrom | Phelan-McDermid syndrom | Dup15Q syndrom | Smith Magenis syndromForente stater
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National Institute of Mental Health (NIMH)FullførtDiGeorge syndrom | Velokardiofacialt syndrom | 22q11.2 syndromForente stater
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Simons SearchlightBoston Children's Hospital; Geisinger Clinic; Simons FoundationRekrutteringSMARCA4 genmutasjon | DDX3X | 16P11.2 Slettingssyndrom | 16p11.2 Duplikasjoner | 1Q21.1 Sletting | 1Q21.1 mikrodupliseringssyndrom (lidelse) | ACTL6B | ADNP | AHDC1 | ANK2 | ANKRD11 | ARID1B | ASH1L | BCL11A | CHAMP1 | CHD2 | CHD8 | CSNK2A1 | CTBP1 | CTNNB1-genmutasjon | CUL3 | DNMT3A | DSCAM | DYRK1A | FOXP1 | GRIN2A | GRIN2B | HIVEP2-relatert intellektuell... og andre forholdForente stater
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Rush University Medical CenterEmory UniversityPåmelding etter invitasjonTuberøs sklerose | Fragilt X-syndrom | Rett syndrom | Hamartoma syndrom, multippel | Angelman syndrom | Kreatinmangel, X-bundet | Telomert 22Q13 Monosomy Syndrome | Kromosom 15Q, delvis slettingForente stater